Anti-cd38 antibodies and formulations

Abstract

Provided herein are antibodies that specifically bind human CD38, formulations and unit dosage forms comprising the antibodies, methods of preparing the antibodies and methods of using the antibodies.

1 . An antibody that specifically binds human CD38, wherein the antibody comprises
 a) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 2 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   b) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 3 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   c) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 4 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   d) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or   e) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9, or   f) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or   g) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9.   
     
     
         2 . A pharmaceutical composition comprising a formulated antibody, wherein the formulated antibody comprises an antibody, sucrose, L-histidine, and polysorbate 80 (PS80), wherein the antibody specifically binds human CD38 and is present at a concentration of 50 mg/mL, the sucrose is present at a concentration of 8% (w/v), the L-histidine is present at a concentration of 10 mM, and the PS80 is present at a concentration of 0.05% (v/v), wherein the formulation has a pH of 6.2, and wherein the antibody comprises
 a) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 2 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   b) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 3 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   c) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 4 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   d) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or   e) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9, or   f) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or   g) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9.   
     
     
         3 . A unit dosage form of a formulated antibody of  claim 1 , wherein the formulated antibody comprises 215 mg of the antibody, 6.21 mg L-histidine, 344 mg sucrose, and 2.15 mg polysorbate 80, wherein the formulated antibody is lyophilized, and wherein the antibody comprises
 a) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 2 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   b) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 3 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   c) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 4 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   d) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or   e) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9, or   f) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or   g) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9.   
     
     
         4 . The pharmaceutical composition of  claim 2 , wherein the formulated antibody is lyophilized or a unit dosage form. 
     
     
         5 . The pharmaceutical composition of  claim 2 , wherein amino acid at position 1 of the HC amino acid sequence is pyroglutamine. 
     
     
         6 . The pharmaceutical composition of  claim 2 , wherein the antibody has an isoelectric point (pI) of 5.8 to 9.0 when measured by capillary isoelectric focusing (cIEF). 
     
     
         7 . The pharmaceutical composition of  claim 2 , wherein the antibody comprises a main charge variant and at least one acidic charge variant and wherein the antibody has at least one of
 a) the HC of the at least one charge variant comprises at least one deamidated asparagine selected from the group consisting of N289, N318, N387, and N392 as numbered according to SEQ ID NO: 1, or   b) the antibody comprises a main charge variant and least one acidic charge variant, wherein the main charge variant comprises at least 71% of the antibody and the acidic charge variant comprises no more than 30% of the antibody, or   c) the main charge variant has an isoelectric point (pI) of 7.5 and wherein the one or more acidic charge variant has pI of 5.8 when measured by capillary isoelectric focusing (cIEF).   
     
     
         8 . The pharmaceutical composition of  claim 2 , wherein the antibody comprises at least one basic charge variant, and wherein the antibody has at least one of
 a) the basic charge variant comprises no more than 4% of the antibody, or   b) the one or more basic charge variants has a pI of 9.0 when measured by capillary isoelectric focusing (cIEF).   
     
     
         9 - 13 . (canceled) 
     
     
         14 . A method for preparing a pharmaceutical composition of  claim 2 , the method comprising the steps of:
 i) expressing the antibody in a cell culture;   ii) subjecting the antibody to at least one purification step selected from the group consisting of chromatography and ultrafiltration to produce a purified antibody solution; and   iii) adjusting the purified antibody solution to produce a formulated antibody comprising
 the purified antibody at a concentration of 50 mg/mL, 
 sucrose at a concentration of 8% w/v, 
 L-histidine at a concentration of 10 mM, and 
 polysorbate 80 at a concentration of 0.05% v/v, 
 wherein the formulated antibody has a pH of 6.2; and 
   iv) lyophilizing the formulated antibody,   thereby preparing the pharmaceutical composition.   
     
     
         15 . A method for preparing a reconstituted formulated antibody of  claim 2  comprising:
 a) providing a lyophilized antibody formulation comprising sucrose, L-histidine, polysorbate 80, and an antibody that specifically binds human CD38; and 
 b) reconstituting the lyophilized antibody formulation in a diluent, wherein the reconstituted antibody formulation comprises
 the antibody at a concentration of 50 mg/mL, 
 sucrose at a concentration of 8% w/v, 
 L-Histidine at a concentration of 10 mM, and 
 polysorbate 80 at a concentration of 0.05% v/v, 
 wherein the reconstituted antibody formulation has a pH of 6.2; 
 wherein the antibody comprises 
 
 i) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 2 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or 
 ii) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 3 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or 
 iii) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 4 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or 
 iv) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or 
 v) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9, or 
 vi) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or 
 vii) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9. 
 
     
     
         16 . A method of treating a patient in need thereof, comprising administering to the patient one or more doses of an antibody that specifically binds human CD38, wherein the patient has a disease that comprises CD38-expessing cells, wherein the antibody comprises
 a) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 2 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   b) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 3 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   c) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 4 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 7, or   d) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or   e) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 5 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9, or   f) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 8, or   g) a heavy chain (HC) having an amino acid sequence of SEQ ID NO: 6 and a light chain (LC) having an amino acid sequence of SEQ ID NO: 9.   
     
     
         17 . (canceled) 
     
     
         18 . The method of  claim 16 , wherein the disease is of hematological origin. 
     
     
         19 . The method of  claim 18 , wherein the disease of hematological origin is selected from the group consisting of: amyloidosis, non-Hodgkin's lymphoma (NHL), Waldenstrom's disease, multiple myeloma (MM), acute lymphocytic leukemia (ALL), and acute myelogenous leukemia (AML). 
     
     
         20 . The method of  claim 16 , wherein the one or more doses of antibody is provided as a lyophilized antibody formulation and wherein prior to administration, the lyophilized antibody formulation is reconstituted forming a reconstituted antibody formulation such that the reconstituted antibody formulation has a pH of 6.2 and comprises the antibody at a concentration of 50 mg/mL in a liquid comprising 10 mM L-histidine, 8% (w/v) sucrose, and 0.05% (v/v) polysorbate 80. 
     
     
         21 . The method of  claim 16 , wherein the antibody is administered at a dose of 20 mg/kg, 10 mg/kg, 5 mg/kg, 3 mg/kg, or 1.5 mg/kg. 
     
     
         22 . The method of  claim 16 , wherein the pharmaceutical composition comprises a formulated antibody, wherein the formulated antibody comprises the antibody present at a concentration of 50 mg/mL, sucrose at a concentration of 8% (w/v), L-histidine at a concentration of 10 mM, and polysorbate 80 (PS80) at a concentration of 0.05% (v/v), wherein the formulated antibody has a pH of 6.2. 
     
     
         23 . The method of  claim 16 , wherein the antibody has an isoelectric point (pI) of 5.8 to 9.0 when measured by capillary isoelectric focusing (cIEF). 
     
     
         24 . The method of  claim 16 , wherein amino acid at position 1 of the HC amino acid sequence is pyroglutamine. 
     
     
         25 . The method of  claim 16 , wherein the antibody comprises a main charge variant and at least one acidic charge variant and wherein the antibody has at least one of
 a) the HC of the at least one charge variant comprises at least one deamidated asparagine selected from the group consisting of N289, N318, N387, and N392 as numbered according to SEQ ID NO: 1, or   b) the antibody comprises a main charge variant and least one acidic charge variant, wherein the main charge variant comprises at least 71% of the antibody and the acidic charge variant comprises no more than 30% of the antibody, or   c) the main charge variant has an isoelectric point (pI) of 7.5 and wherein the one or more acidic charge variant has pI of 5.8 when measured by capillary isoelectric focusing (cIEF).   
     
     
         26 . The method of  claim 16 , wherein the antibody comprises at least one basic charge variant, and wherein the antibody has at least one of
 a) the basic charge variant comprises no more than 4% of the antibody, or   b) the one or more basic charge variants has a pI of 9.0 when measured by capillary isoelectric focusing (cIEF).